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PLASTICS – DETERMINATION OF THE TOTAL LUMINOUS TRANSMITTANCE OF TRANSPARENT MATERIALS – PART 1: SINGLE-BEAM INSTRUMENT (ISO 13468-1:1996, IDT)
MS ISO 13468-1:2004
Status : Withdrawn
Format : PDF

This Malaysian Standard covers the determination of the total luminous transmittance, in the visible region of the spectrum, of planar transparent and substantially colourless plastics, using a Single ....Read more -beam photometer with a specified CIE Standard light Source and photodetector. This part of ISO 13468 cannot be used for plastics which contain fluorescent materials. 
This part of ISO 13468 is applicable to transparent moulding materials, films and sheets not exceeding 10 mm in thickness.

NOTES

1 Total luminous transmittance tan also be determined by a double-beam spectrophotometer as in part 2 of the standard. Part 1, however, provides a simple but precise, practical and quick determination. This method is suitable for use not only for analytical purposes but also for quality control.

2 Substantially colourless plastics include those which are faintly tinted.

3 Specimens more than 10 mm thick may be measured provided the instrument tan accommodate them, but the results may not be Close

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PLASTICS - DETERMINATION OF THE TOTAL LUMINOUS TRANSMITTANCE OF TRANSPARENT MATERIALS - PART 2: DOUBLE-BEAM INSTRUMENT (ISO 13468-2:1999, IDT)
MS ISO 13468-2:2004 (CONFIRMED:2011)
Status : 1st Confirmation
Format : PDF

This Malaysian Standard covers the determination of the total luminous transmittance, in the visible region of the spectrum, of planar transparent and substantially colourless plastics, using a double ....Read more -beam scanning spectrophotometer. This standard cannot be used for plastics which contain fluorescent materials. Close

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Steel wire rope slings - Safety - Part 2: Specification for information for use and maintenance to be provided by the manufacturer
MS EN 13414-2:2012
Status : Original
Format : PDF

This Malaysian Standard specifies the information on use and maintenance to be provided by the manufacturer of wire rope slings.

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Steel wire rope slings - Safety - Part 3: Grommets and cable-laid slings
MS EN 13414-3:2012
Status : Original
Format : PDF

This Malaysian Standard specifies the construction requirements, calculation of WLL, testing and certification of steel wire rope grommets, cable-laid grommets and cable-laid slings using strand and w ....Read more ire rope conforming to EN 12385-4. Close

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Steel wire rope slings - Safety - Part 1: Slings for general lifting service
MS EN 13414-1:2012
Status : Original
Format : PDF

This Malaysian Standard specifies the construction requirements, calculation of WLL, verification, certification and marking of steel wire rope slings for general lifting service. It covers single-, t ....Read more wo-, three- and four-leg slings, with ferrule-secured or spliced eye terminations and sliced or ferrule-secured endless slings made from 8 mm to 60 mm diameter strand ordinary lay steel wire rope with fibre or steel core and 8 strand ordinary lay steel wire rope with a steel core conforming to EN 12385-4. Close

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ASEPTIC PROCESSING OF HEALTH CARE PRODUCTS - PART 5: STERILIZATION IN PLACE (ISO 13408-5:2006, IDT)
MS ISO 13408-5:2010 (CONFIRMED:2020)
Status : Original
Format : PDF

This Malaysian Standard specifies the general requirements for sterilization in place (SIP) applied to product contact surfaces of the equipment used in the manufacture of sterile health care products ....Read more by aseptic processing and offers guidance on qualification, validation, operation and control. 
This Malaysian Standard applies to processes where sterilizing agents are delivered to the internal surfaces of equipment that can come in contact with the product.

This standard does not apply to processes where equipment is dismantled and delivered to a
sterilizer.

This standard does not supersede or replace national regulatory requirements, such as Good Manufacturing Practices (GMPs) and/or compendial requirements that pertain in particular national or regional jurisdictions.

This standard does not specify requirements for development, validation and routine control of a
process for inactivating the causative agents of spongiform encephalopathies, such as scrapie, bovine spongiform e Close

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Aseptic processing of health care products - Part 1: General requirements (ISO 13408-1:2008, IDT)
MS ISO 13408-1:2011 (CONFIRMED:2020)
Status : Original
Format : PDF

This Malaysian Standard specifies the general requirements for, and offers guidance on, processes, programmes and procedures for development, validation and routine control of the manufacturing proces ....Read more s for aseptically-processed health care products. 
This standard includes requirements and guidance relative to the overall topic of aseptic processing. Specific requirements and guidance on various specialized processes and methods related to filtration, lyophilization, clean-in place (CIP) technologies, sterilization in place (SIP) and isolator systems are given in other parts of MS ISO 13408. Close

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Aseptic processing of health care products - Part 6: Isolator systems (ISO 13408-6:2005, IDT)
MS ISO 13408-6:2011
Status : Original
Format : PDF

This Malaysian Standard specifies the requirements for isolator systems used for aseptic processing and offers guidance on qualification, bio-decontamination, validation, operation and control of isol ....Read more ator systems used for aseptic processing of health care products. 
This standard is focused on the use of isolator systems to maintain aseptic conditions; this may include applications for hazardous materials. Close

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Aseptic processing of health care products - Part 2: Filtration (ISO 13408-2:2003, IDT)
MS ISO 13408-2:2011
Status : Original
Format : PDF

This Malaysian Standard specifies requirements for sterilizing filtration as part of aseptic processing of health care products. It also offers guidance to filter users concerning general requirements ....Read more for set-up, validation and routine operation of a sterilizing filtration process, to be used for aseptic processing of health care products. 
This Malaysian Standard is not applicable to removal of viruses. Sterilizing filtration is not applicable to fluids containing particles as effective ingredient larger than the pore size of a filter (e.g. bacterial whole-cell vaccines). Close

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Aseptic processing of health care products - Part 3: Lyophilization (ISO 13408-3:2006, IDT)
MS ISO 13408-3:2011 (CONFIRMED:2020)
Status : Original
Format : PDF

This Malaysian Standard specifies requirements for, and offers guidance on, equipment, processes, programmes and procedures for the control and validation of lyophilization as an aseptic process. It d ....Read more oes not address the physical/chemical objectives of a lyophilization process. Close

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